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Sequential treatment with 5‐aza‐2′‐deoxycytidine and deacetylase inhibitors reactivates HIV‐1
Reactivation of HIV gene expression in latently infected cells together with an efficient cART has been proposed as an adjuvant therapy aimed at eliminating/decreasing the reservoir size. Results from HIV clinical trials using deacetylase inhibitors (HDACIs) question the efficiency of these latency‐...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734845/ https://www.ncbi.nlm.nih.gov/pubmed/26681773 http://dx.doi.org/10.15252/emmm.201505557 |
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author | Bouchat, Sophie Delacourt, Nadège Kula, Anna Darcis, Gilles Van Driessche, Benoit Corazza, Francis Gatot, Jean‐Stéphane Melard, Adeline Vanhulle, Caroline Kabeya, Kabamba Pardons, Marion Avettand‐Fenoel, Véronique Clumeck, Nathan De Wit, Stéphane Rohr, Olivier Rouzioux, Christine Van Lint, Carine |
author_facet | Bouchat, Sophie Delacourt, Nadège Kula, Anna Darcis, Gilles Van Driessche, Benoit Corazza, Francis Gatot, Jean‐Stéphane Melard, Adeline Vanhulle, Caroline Kabeya, Kabamba Pardons, Marion Avettand‐Fenoel, Véronique Clumeck, Nathan De Wit, Stéphane Rohr, Olivier Rouzioux, Christine Van Lint, Carine |
author_sort | Bouchat, Sophie |
collection | PubMed |
description | Reactivation of HIV gene expression in latently infected cells together with an efficient cART has been proposed as an adjuvant therapy aimed at eliminating/decreasing the reservoir size. Results from HIV clinical trials using deacetylase inhibitors (HDACIs) question the efficiency of these latency‐reversing agents (LRAs) used alone and underline the need to evaluate other LRAs in combination with HDACIs. Here, we evaluated the therapeutic potential of a demethylating agent (5‐AzadC) in combination with clinically tolerable HDACIs in reactivating HIV‐1 from latency first in vitro and next ex vivo. We showed that a sequential treatment with 5‐AzadC and HDACIs was more effective than the corresponding simultaneous treatment both in vitro and ex vivo. Interestingly, only two of the sequential LRA combinatory treatments tested induced HIV‐1 particle recovery in a higher manner than the drugs alone ex vivo and at concentrations lower than the human tolerable plasmatic concentrations. Taken together, our data reveal the benefit of using combinations of 5‐AzadC with an HDACI and, for the first time, the importance of treatment time schedule for LRA combinations in order to reactivate HIV. |
format | Online Article Text |
id | pubmed-4734845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47348452016-02-09 Sequential treatment with 5‐aza‐2′‐deoxycytidine and deacetylase inhibitors reactivates HIV‐1 Bouchat, Sophie Delacourt, Nadège Kula, Anna Darcis, Gilles Van Driessche, Benoit Corazza, Francis Gatot, Jean‐Stéphane Melard, Adeline Vanhulle, Caroline Kabeya, Kabamba Pardons, Marion Avettand‐Fenoel, Véronique Clumeck, Nathan De Wit, Stéphane Rohr, Olivier Rouzioux, Christine Van Lint, Carine EMBO Mol Med Research Articles Reactivation of HIV gene expression in latently infected cells together with an efficient cART has been proposed as an adjuvant therapy aimed at eliminating/decreasing the reservoir size. Results from HIV clinical trials using deacetylase inhibitors (HDACIs) question the efficiency of these latency‐reversing agents (LRAs) used alone and underline the need to evaluate other LRAs in combination with HDACIs. Here, we evaluated the therapeutic potential of a demethylating agent (5‐AzadC) in combination with clinically tolerable HDACIs in reactivating HIV‐1 from latency first in vitro and next ex vivo. We showed that a sequential treatment with 5‐AzadC and HDACIs was more effective than the corresponding simultaneous treatment both in vitro and ex vivo. Interestingly, only two of the sequential LRA combinatory treatments tested induced HIV‐1 particle recovery in a higher manner than the drugs alone ex vivo and at concentrations lower than the human tolerable plasmatic concentrations. Taken together, our data reveal the benefit of using combinations of 5‐AzadC with an HDACI and, for the first time, the importance of treatment time schedule for LRA combinations in order to reactivate HIV. John Wiley and Sons Inc. 2015-12-17 2016-02 /pmc/articles/PMC4734845/ /pubmed/26681773 http://dx.doi.org/10.15252/emmm.201505557 Text en © 2015 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Bouchat, Sophie Delacourt, Nadège Kula, Anna Darcis, Gilles Van Driessche, Benoit Corazza, Francis Gatot, Jean‐Stéphane Melard, Adeline Vanhulle, Caroline Kabeya, Kabamba Pardons, Marion Avettand‐Fenoel, Véronique Clumeck, Nathan De Wit, Stéphane Rohr, Olivier Rouzioux, Christine Van Lint, Carine Sequential treatment with 5‐aza‐2′‐deoxycytidine and deacetylase inhibitors reactivates HIV‐1 |
title | Sequential treatment with 5‐aza‐2′‐deoxycytidine and deacetylase inhibitors reactivates HIV‐1 |
title_full | Sequential treatment with 5‐aza‐2′‐deoxycytidine and deacetylase inhibitors reactivates HIV‐1 |
title_fullStr | Sequential treatment with 5‐aza‐2′‐deoxycytidine and deacetylase inhibitors reactivates HIV‐1 |
title_full_unstemmed | Sequential treatment with 5‐aza‐2′‐deoxycytidine and deacetylase inhibitors reactivates HIV‐1 |
title_short | Sequential treatment with 5‐aza‐2′‐deoxycytidine and deacetylase inhibitors reactivates HIV‐1 |
title_sort | sequential treatment with 5‐aza‐2′‐deoxycytidine and deacetylase inhibitors reactivates hiv‐1 |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734845/ https://www.ncbi.nlm.nih.gov/pubmed/26681773 http://dx.doi.org/10.15252/emmm.201505557 |
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